Company Description At TAPI we re not just a company we re a community committed to advancing health from the core As the world s leading supplier of active pharmaceutical ingredients APIs we partner with 80 of the top 50 global pharmaceutical companies With a legacy spanning over 80 years and a portfolio of more than 350 products as well as custom CDMO services we re shaping the future of health worldwide Our strength lies in our people a team of over 4 200 professionals across 13 state-of-the-art facilities in Italy Hungary the Czech Republic Croatia Israel Mexico and India Together we innovate solve problems and deliver excellence Join us and be part of a mission that transforms lives We re looking for a detail-driven Quality Control QC Technician with a strong foundation in GMP GLP compliance analytical testing and audit readiness If you excel in 24 7 audit preparedness regulatory documentation instrument calibration and hands-on analysis of raw materials intermediates and environmental samples this role offers a dynamic lab environment to thrive in You ll lead investigations LIR OOS OOT ensure data integrity support CAPA training and drive QC efficiency through meticulous documentation 5S practices and cross-functional coordination Main Responsibilities 24 x 7 audit readiness Participation in internal external regulatory audits Ensure 100 participation in training s against CAPA s Responsible for initiation and investigation on LIR OOS OOT boarder line results and reporting them to the in-charge Supporting to share required documents from QC to RA another requirement Determining team priorities in accordance with the plant s needs while coordinating with the team leader Manger Follow up the housekeeping cGMP GLP and Safety Guideline in laboratory Sampling analysis planning of RM PG intermediates water Environment monitoring samples based on requirement and result entry in analytical sheets QA form and LIMS Perform analytical test according to the monograph and SOP based on requirement in different shifts A B and C Signing on approved column in data books laboratory control card and signing on hard copies as well as approval in LIMS based on requirement Responsible for calibration and verification of instruments Maintaining of reserved samples room and chambers Help in preparation of documents related to department like STP s SOP s etc Ensure the sampling of finished products Raw material Intermediate and sending sample to outside laboratory for analysis Must be ensured sampled approved and rejected labels timely as required Responsible for maintaining the stock record of chemicals and reconciliation of standards Responsible for maintaining safety CAPA Responsible for maintaining 5-S in QC Online documentation based on requirement must be ensured as per data integrity norms and awareness to team against data integrity Responsible for support analysis reduction QC efficiency enhancement programs Any other job assigned by the Manger -QC Manger or group leader-QC Qualifications The ideal candidate will have Education B Sc M Sc in Chemistry Experience Minimum 6 years of industrial experience Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job it s an prospect to make a lasting impact on global health If you re ready to lead innovate and inspire we re excited to welcome you to our team Together let s shape the future of pharmaceuticals Apply on top of this page and our talent acquisition team will be in touch soon

📌 Quality Control Technician (Malanpur)
🏢 Tapi
📍 Malanpur